GapMind for catabolism of small carbon sources

 

L-lysine catabolism in Pandoraea thiooxydans ATSB16

Best path

lysP, cadA, patA, patD, davT, davD, gcdG, gcdH, ech, fadB, atoB

Rules

Overview: Lysine degradation in GapMind is based on many metacyc pathways (link), including L-lysine degradation I via cadaverine (link), pathway IV via lysine monooxygenase (link), pathway V via D-lysine (link), pathway VI via lysine 6-aminotransferase (link), pathway VIII via lysine 6-dehydrogenase (link), and fermentation to acetate and butanoate (link). Pathway X (link) is similar to pathway I (with cadaverine and glutarate as intermediates), but glutarate is consumed via glutaryl-CoA (as in pathway IV); it does not introduce any new steps. Pathways II (L-pipecolate pathway) and III (via N6-acetyllysine) and VII (via 6-amino-2-oxohexanoate) and IX (similar to pathway IV) and XI (via saccharopine) are not thought to occur in prokaryotes and are not included in GapMind.

44 steps (32 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
lysP L-lysine:H+ symporter LysP PATSB16_RS09985 PATSB16_RS02760
cadA lysine decarboxylase PATSB16_RS03825 PATSB16_RS04280
patA cadaverine aminotransferase PATSB16_RS01925 PATSB16_RS17895
patD 5-aminopentanal dehydrogenase PATSB16_RS14485 PATSB16_RS01930
davT 5-aminovalerate aminotransferase PATSB16_RS10400 PATSB16_RS17895
davD glutarate semialdehyde dehydrogenase PATSB16_RS01900 PATSB16_RS01105
gcdG succinyl-CoA:glutarate CoA-transferase PATSB16_RS12580 PATSB16_RS17175
gcdH glutaryl-CoA dehydrogenase PATSB16_RS01745 PATSB16_RS16800
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase PATSB16_RS20735 PATSB16_RS06150
fadB (S)-3-hydroxybutanoyl-CoA dehydrogenase PATSB16_RS15750 PATSB16_RS16980
atoB acetyl-CoA C-acetyltransferase PATSB16_RS05650 PATSB16_RS05675
Alternative steps:
alr lysine racemase
amaA L-pipecolate oxidase PATSB16_RS14990
amaB L-2-aminoadipate semialdehyde dehydrogenase (AmaB/Pcd) PATSB16_RS19575 PATSB16_RS01105
amaD D-lysine oxidase PATSB16_RS07030
argT L-lysine ABC transporter, substrate-binding component ArgT PATSB16_RS05365 PATSB16_RS18535
bcd butanoyl-CoA dehydrogenase (NAD+, ferredoxin), dehydrogenase subunit PATSB16_RS16820 PATSB16_RS16800
bgtB L-histidine ABC transporter, fused substrate-binding and permease components (BgtB/BgtAB)
ctfA butanoyl-CoA:acetoacetate CoA-transferase, alpha subunit PATSB16_RS12320 PATSB16_RS11255
ctfB butanoyl-CoA:acetoacetate CoA-transferase, beta subunit PATSB16_RS12315 PATSB16_RS11250
davA 5-aminovaleramidase PATSB16_RS03930
davB L-lysine 2-monooxygenase
dpkA 1-piperideine-2-carboxylate reductase PATSB16_RS12815 PATSB16_RS18950
etfA butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfA subunit PATSB16_RS12955
etfB butanoyl-CoA dehydrogenase (NAD+, ferredoxin), etfB subunit PATSB16_RS12960
glaH glutarate 2-hydroxylase, succinate-releasing (GlaH or CsiD)
hglS D-2-hydroxyglutarate synthase
hisM L-lysine ABC transporter, permease component 1 (HisM) PATSB16_RS13415 PATSB16_RS05360
hisP L-lysine ABC transporter, ATPase component HisP PATSB16_RS15000 PATSB16_RS15715
hisQ L-lysine ABC transporter, permease component 2 (HisQ) PATSB16_RS10375 PATSB16_RS05360
kal 3-aminobutyryl-CoA deaminase
kamA L-lysine 2,3-aminomutase
kamD L-beta-lysine 5,6-aminomutase, alpha subunit
kamE L-beta-lysine 5,6-aminomutase, beta subunit
kce (S)-5-amino-3-oxohexanoate cleavage enzyme PATSB16_RS07855 PATSB16_RS17900
kdd 3,5-diaminohexanoate dehydrogenase
lat L-lysine 6-aminotransferase PATSB16_RS01925 PATSB16_RS01020
lhgD L-2-hydroxyglutarate dehydrogenase or oxidase (LhgD or LhgO) PATSB16_RS14805
LHT L-lysine transporter
lysDH L-lysine 6-dehydrogenase PATSB16_RS04490 PATSB16_RS02085
lysL L-lysine transporter LysL PATSB16_RS06030
lysN 2-aminoadipate transaminase PATSB16_RS18960 PATSB16_RS04790
Slc7a1 L-lysine transporter Slc7a1
ydiJ (R)-2-hydroxyglutarate dehydrogenase PATSB16_RS12390 PATSB16_RS08560

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory